Molecular Characterization of Aminoglycoside-modifying Enzymes (AMEs)in Aminoglycoside-Resistant Staphylococcus

Malihe Naderi1,2, Neda Yousefi Nojookambari3, Somayeh Talebi1

  • 1Infectious Diseases Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

PubMed
Abstract

Insights

Aminoglycoside resistance genes are common in Staphylococcus aureus clinical isolates. The study found high rates of resistance and prevalent AME genes, including aac(6')/aph(2'), raising concerns for treatment options.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Infectious Diseases

Background:

  • Aminoglycoside-modifying enzyme (AME) encoding genes are increasingly prevalent in Staphylococcus aureus.
  • Understanding the frequency of these resistance genes in clinical isolates is crucial.

Purpose of the Study:

  • To determine the prevalence of AME-encoding genes in clinical Staphylococcus aureus isolates.
  • To characterize antibiotic resistance patterns and identify specific resistance genes.

Main Methods:

  • Conventional biochemical tests for S. aureus identification.
  • Agar disk diffusion for antibiotic resistance profiling.
  • Conventional and multiplex PCR for detecting AME and femA genes.

Main Results:

  • High aminoglycoside resistance rates observed for kanamycin (47.6%), tobramycin (46.6%), gentamicin (45.7%), and amikacin (45.7%).
  • The aac(6")/aph(2") gene was the most prevalent AME gene (47.8%), followed by ant(4">-Ia (30.4%) and aph(3">-IIIa (21.7%).
  • The femA gene was present in 21.9% of isolates, associated with methicillin-resistant S. aureus (MRSA).

Conclusions:

  • The widespread presence of AME genes and femA in S. aureus clinical isolates is concerning.
  • This resistance can broaden aminoglycoside resistance and limit treatment options for staphylococcal infections.